Ultrasonic handpiece

ABSTRACT

An ultrasonic handpiece includes a horn and a transducer system. The transducer system is configured to detect a first pressure applied to at least a first portion of the transducer system, transmit a signal associated with the first pressure, and generate ultrasonic vibratory energy. The first pressure is associated with a second pressure applied to the horn.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Patent ApplicationNo. 61/496,147 filed Jun. 13, 2011, U.S. Provisional Patent ApplicationNo. 61/526,182 filed Aug. 22, 2011, and U.S. Provisional PatentApplication No. 61/526,207 filed Aug. 22, 2011, which are herebyincorporated by reference in their respective entireties.

BACKGROUND

The present disclosure relates generally to medical devices and, moreparticularly, to an ultrasonic handpiece.

Various types of known medical procedures involve repair andstabilization of body tissue. Such medical procedures may be utilized,for example, to treat conditions, such as, without limitation, a defect,damage, or fracture to bone, damaged or torn muscle, ligament or tendon,or separation of body tissues, etc. For example, fractured bones ofteninvolve stabilization of the bone in order to promote healing. Differentbones and/or different types of fractures generally require uniqueprocedures and/or surgical implements to facilitate stabilization of thebody tissue. Accordingly, medical personnel employ a variety of surgicalimplements, such as screws, plates, and rods, to stabilize the boneacross the fracture. In another example, further surgical implements maybe used to anchor torn ligaments or tendons to other appropriate bodytissue. As such, a variety of medical procedures and surgical implementsare known to be used within the body of a patient to facilitate repair,stabilization, and/or healing of body tissue.

BRIEF SUMMARY

In one aspect, a method is provided for operating a handheld medicaldevice. The method includes detecting a first pressure applied to aforce determining mechanism. The first pressure is associated with asecond pressure applied to a horn. The method further includestransmitting a signal associated with the first pressure, and generatingvibratory energy based at least in part on the first pressure.

In another aspect, a medical device is provided. The medical deviceincludes a vibrating mechanism, a horn, and a force determiningmechanism. The vibrating mechanism is configured to generate vibratoryenergy. The horn is configured to transmit the vibratory energygenerated by the vibrating mechanism to an operative site. The forcedetermining mechanism is configured to detect a first pressure appliedto the force determining mechanism and transmit a signal associated withthe first pressure. The first pressure is associated with a secondpressure applied to the horn.

In yet another aspect, an ultrasonic handpiece is provided. Theultrasonic handpiece includes a horn and a transducer system. Thetransducer system is configured to detect a first pressure applied to atleast a first portion of the transducer system, transmit a signalassociated with the first pressure, and generate ultrasonic vibratoryenergy. The first pressure is associated with a second pressure appliedto the horn.

The features, functions, and advantages described herein may be achievedindependently in various embodiments of the present disclosure or may becombined in yet other embodiments, further details of which may be seenwith reference to the following description and drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1-4 show exemplary embodiments of the methods and systemsdescribed herein.

FIG. 1 is a schematic illustration of an exemplary surgical system;

FIG. 2 is a cross-sectional view of an exemplary ultrasonic handpiecethat may be used with the surgical system shown in FIG. 1;

FIG. 3 is a flowchart of an exemplary method of operating the surgicalsystem shown in FIG. 1; and

FIG. 4 is a cross-sectional view of another exemplary ultrasonichandpiece that may be used with the surgical system shown in FIG. 1.

Although specific features of various embodiments may be shown in somedrawings and not in others, this is for convenience only. Any feature ofany drawing may be referenced and/or claimed in combination with anyfeature of any other drawing.

DETAILED DESCRIPTION

The present disclosure relates generally to medical devices and, moreparticularly, to ultrasonic handpieces. In one embodiment, an ultrasonichandpiece includes a vibrating mechanism, a horn, and a forcedetermining mechanism. The force determining mechanism detects a forceand/or pressure applied to the force determining mechanism, andtransmits a first signal associated with the force and/or pressure to asurgical generator. The surgical generator transmits a second signal tothe vibrating mechanism based on the first signal to generate vibratoryenergy, which is transmitted by the horn to an operative site.

As used herein, an element or step recited in the singular and precededwith the word “a” or “an” should be understood as not excluding pluralelements or steps unless such exclusion is explicitly recited. Moreover,references to “one embodiment” and/or the “exemplary embodiment” are notintended to be interpreted as excluding the existence of additionalembodiments that also incorporate the recited features.

FIG. 1 shows an exemplary surgical system 100 including a surgicalgenerator 110 and a handpiece 120, which may be removably coupled tosurgical generator 110. Alternatively, surgical generator 110 may beintegrated with handpiece 120. As used herein, surgical and/or surgeryare used to generally refer to any medical procedure involving a patient(a human being, an animal, etc.) and may include in-patient procedures,out-patient procedures, invasive procedures, non-invasive procedures,and/or minimally invasive procedures. In at least some embodiments,surgical implements (not shown) are disposed within the patient's bodyin orientations suitable for a respective medical procedure, such as afracture stabilization procedure. Surgical implements may includeimplants or other suitable medical devices such as, without limitation,pins, screws, fasteners, dowels, rods, plates, and/or anchors. Moreover,as used herein, handpiece is used to generally refer to a housing,casing, frame, holder, and/or support that can be manually carried andmanipulated during a medical procedure involving a patient.

In the exemplary embodiment, surgical generator 110 includes aprocessing device 130 and a memory device 140 coupled to processingdevice 130. Processing device 130 may include, without limitation, amicrocontroller, a microprocessor, a programmable gate array, anapplication specific integrated circuit (ASIC), a logic circuit, and/orany other circuit, integrated or otherwise, suitable to perform asdescribed herein. Memory device 140 includes one or more devicesoperable to enable information such as executable instructions and/orother data to be stored and/or retrieved. Memory device 140 may includeone or more computer readable media including, without limitation, harddisk storage, optical drive/disk storage, removable disk storage, flashmemory, non-volatile memory, ROM, electrically-erasable programmableread-only memory (EEPROM), and/or random access memory (RAM). Memorydevice 140 is used to store one or more of predetermined thresholds,resonant frequencies, settings specific to handpiece 120, and/orexecutable instructions.

In the exemplary embodiment, surgical generator 110 includes an outputdevice 150 for example, a cathode ray tube (CRT), a liquid crystaldisplay (LCD), an LED display, an “electronic ink” display, and/or otherdevice suitable to display information to an operator. Additionally,output device 150 may include an audio output device (e.g., a speaker,etc.) to indicate verbal instructions, alerts, and/or warnings to theoperator.

In the exemplary embodiment, surgical generator 110 includes one or moreinput devices, such as, without limitation, a button, a pedal, a knob, akeypad, a pointing device, a mouse, a touch sensitive panel (e.g., atouch pad or a touchscreen), a gyroscope, a position detector, and/or anaudio input (e.g., a microphone). For example, in the exemplaryembodiment, a foot pedal 160 is removably coupled to surgical generator110 to enable an operator to provide input to surgical generator 110. Inone embodiment, the input device is integrated with surgical generator110. In another embodiment, the input device is remote from surgicalgenerator 110 and coupled thereto.

Different types of handpieces 120 may be used with surgical generator110 based on a type of medical procedure and/or a type of surgicalimplement. For example, various handpieces 120 may have differentconfigurations and/or properties (e.g., acoustical characteristics,resonance frequency), and/or various surgical implements may requirehandpieces 120 of different sizes and/or configurations. In theexemplary embodiment, an identifier (not shown) enables surgicalgenerator 110 to automatically identify handpiece 120. For example,surgical generator 110 may read and/or detect a resistanceidentification, an RFID tag, and/or another identifying component todifferentiate handpiece 120 from other handpieces 120. Additionally oralternatively, an operator may manually identify handpiece 120. In atleast some embodiments, the identifier is associated with multiplemedical procedures and/or surgical implements. In such embodiments, theoperator may provide, and surgical generator 110 may receive, one ormore inputs to select a medical procedure to be performed and/or asurgical implement to be interfaced.

In this manner, one or more handpieces 120 may be replaced betweenmedical procedures. In at least some embodiments, handpiece 120 isremoved after each patient such that handpiece 120 may be autoclavedbetween medical procedures to substantially ensure sterility for one ormore subsequent patients. Accordingly, handpiece 120 is configured towithstand multiple autoclave procedures.

In the exemplary embodiment, handpiece 120 includes an outer housing170, a horn 180 extending longitudinally from outer housing 170, an endeffector 190 coupled to horn 180, and a sheath 195 (shown in FIG. 2)coupled to outer housing 170 and extending about and spaced radiallyfrom horn 180 and/or end effector 190. In the exemplary embodiment, horn180 and/or end effector 190 are sized and/or configured to slide withinsheath 195. In at least some embodiments, end effector 190 is integratedwith horn 180.

In the exemplary embodiment, handpiece 120 is useable to affect one ormultiple surgical implements during a surgery. More specifically,handpiece 120 applies vibratory energy, such as ultrasonic energy, toone or more of the surgical implements to form a weld between thesurgical implements. Alternatively, handpiece 120 may apply any energythat enables surgical generator 110 and/or handpiece 120 to function asdescribed herein.

In the exemplary embodiment, handpiece 120 is configured to provide anergonomic interaction with an operator including, without limitation, asurgeon, a doctor, a surgery assistant, a nurse, a veterinarian, and/orother medical personnel present for a medical procedure. Other shapesand/or sizes of handpiece 120 may be included in other surgical systemembodiments. In at least some embodiments, handpiece 120 is configuredto interact with and/or be utilized by a robotic and/or haptic arm forrobotic (e.g., fully automatic or programmed) and/or remote control(e.g., direct human control with end points or boundaries) of handpiece120.

FIG. 2 is a cross-sectional view of handpiece 120. In the exemplaryembodiment, outer housing 170 houses at least an inner housing 200 andat least a portion of a transducer system or, more specifically, loadcell 210. In the exemplary embodiment, load cell 210 is configured todetect a first force and/or pressure applied to load cell 210 andtransmit to surgical generator 110 (shown in FIG. 1) a pressure signalassociated with and/or indicative of the first pressure. The firstpressure is associated with a force and/or pressure between end effector190 (shown in FIG. 1) and a surgical implement in contact with endeffector 190, which, in turn, directly applies a force and/or pressureto horn 180.

In the exemplary embodiment, a biasing mechanism 220 is positionedwithin outer housing 170 to counteract, reduce and/or limit the firstpressure applied to load cell 210. More specifically, biasing mechanism220 is moveable between an unflexed or home position and a flexedposition. In this manner, load cell 210 “floats” within outer housing170. As the first pressure applied to load cell 210 generally increases,in the exemplary embodiment, biasing mechanism 220 moves toward theflexed position. Conversely, as the first pressure applied to load cell210 generally decreases, in the exemplary embodiment, biasing mechanism220 moves toward the home position. In the exemplary embodiment, biasingmechanism 220 includes a spring plate 230 and a wave spring 240 that isconfigured to compress as the first pressure increases and/or expand asthe first pressure decreases. Alternatively, any type of biasingmechanism 220 may be used that enables handpiece 120 to function asdescribed herein. In at least some embodiments, load cell 210 is fixedlycoupled within outer housing 170.

In the exemplary embodiment, outer housing 170 defines a cavity thereinthat is sized and/or configured such that inner housing 200 is retainedwithin outer housing 170. More specifically, outer housing 170 and/orinner housing 200 includes at least one retaining mechanism 250 thatfacilitates counteracting, reducing, and/or limiting the first pressureapplied to load cell 210. For example, in the exemplary embodiment,retaining mechanism 250 is positioned within outer housing 170 betweeninner housing 200 and load cell 210 to prevent and/or limit innerhousing 200 from moving toward load cell 210 beyond a predeterminedposition. In the exemplary embodiment, a portion of retaining mechanism250 is positioned at the predetermined position within a groove 260defined by an inner surface of outer housing 170. In the exemplaryembodiment, retaining mechanism 250 includes an opening 270 extendinglongitudinally therethrough, and a standoff 280 coupled to inner housing200 extends through opening 270 such that standoff 280 is configured todirectly apply the first pressure to load cell 210. In at least someembodiments, standoff 280 may be a spring. Alternatively, any type ofretaining mechanism 250 and/or standoff 280 may be used that enableshandpiece 120 to function as described herein.

In the exemplary embodiment, inner housing 200 houses at least a portionof horn 180 and at least a portion of the transducer system or, morespecifically, vibrating mechanism 290 coupled to horn 180. In theexemplary embodiment, vibrating mechanism 290 is a piezoelectric stackthat is configured to generate vibratory energy (e.g., ultrasonicenergy) upon receiving a control signal to activate a weld cycle. In theexemplary embodiment, horn 180 is configured to transmit the vibratoryenergy to an operative site. More specifically, horn 180 is coupleableto end effector 190 such that the vibratory energy is transmitted to endeffector 190 through horn 180. Alternatively, the vibratory energy maybe transmitted to the operative site using any mechanism that enableshandpiece 120 to function as described herein.

The transducer system includes at least vibrating mechanism 290 and loadcell 210. In this manner, the transducer system is configured to detectthe first pressure, transmit the pressure signal, and generateultrasonic vibratory energy. In the exemplary embodiment, vibratingmechanism 290 is remote from load cell 210. Alternatively, vibratingmechanism 290 may be adjacent and/or integrated with load cell 210, orload cell 210 may be adjacent and/or integrated with vibrating mechanism290. For example, the first pressure may be determined based on apressure detected by vibrating mechanism 290, and/or load cell 210 maybe configured to generate vibratory energy.

In at least some embodiments, handpiece 120 includes a series ofelectrical contacts that are coupled to vibrating mechanism 290. In suchembodiments, the electrical contacts are moveable between a closedconfiguration and an open configuration such that the electricalcontacts are electrically and/or communicatively coupled and/ordecoupled, respectively. In such embodiments, as pressure applied to endeffector 190, horn 180, and/or load cell 210 generally increases, theelectrical contacts move toward the closed configuration, therebycoupling surgical generator 110 to vibrating mechanism 290. Conversely,as pressure applied to end effector 190, horn 180, and/or load cell 210generally decreases, in such embodiments, the electrical contacts movetoward the open configuration, thereby decoupling surgical generator 110from vibrating mechanism 290. Alternatively, the electrical contacts maybe positioned anywhere within handpiece 120 that enables surgical system100 to function as described herein.

FIG. 3 is a flowchart of an exemplary method 300 of operating surgicalsystem 100. During operation, in the exemplary embodiment, handpiece 120is identified based on an identifier and/or selected based on a type ofmedical procedure and/or surgical implement. In the exemplaryembodiment, surgical generator 110 retrieves one or more settingsassociated with handpiece 120, the medical procedure, and/or thesurgical implement from memory device 140 based on the identifier. Thesettings are used by surgical generator 110 to provide one or morecontrol signals to handpiece 120. Settings retrieved from memory device140 may include, without limitation, frequencies, voltages, currents,and/or control algorithms. For example, in the exemplary embodiment, thesetting retrieved from memory device 140 includes a predetermined firstforce and/or pressure range that enables vibratory energy transfer tothe surgical implement, as described below.

Upon identification and/or selection of handpiece 120 and retrieval ofone or more settings from memory device 140, surgical system 100 isgenerally ready to affect the surgical implement. In the exemplaryembodiment, end effector 190 is positioned 310 at least partially withinthe patient and in contact with the surgical implement. Morespecifically, the operator uses handpiece 120 to apply force and/orpressure to the surgical implement, which, in turn, applies a forceand/or pressure to horn 180 and inner housing 200. As a result, standoff280 applies the first pressure to load cell 210, which detects 320 thefirst pressure and transmits 330 the pressure signal from handpiece 120to surgical generator 110.

In at least some embodiments, output device 150 presents an indicationof the pressure to the operator. For example, in one embodiment, avisual display presents a visual indication of the applied pressurerelative to the first pressure range such that the operator is able tovisualize what, if any, corrections need to be made in order to providea pressure within the first pressure range. Additionally oralternatively, an audio output device presents an audible toneindicative of the applied pressure, and/or a tactile output devicepresents vibrations indicative of the applied pressure. The tone and/orvibrations may include three rates, volumes, and/or intensities: a firstrate, volume, and/or intensity indicating the pressure is below thefirst pressure range, a second rate, volume, and/or intensity indicatingthe pressure is within the first pressure range, and a third rate,volume, and/or intensity indicating the pressure is above the firstpressure range. As such, the audible tone and/or the vibrations enablethe operator to understand the applied pressure relative to the firstpressure range without diverting the operator's visual attention fromthe patient and/or surgical implement.

In the exemplary embodiment, when the pressure is below the firstpressure range, output device 150 presents no visual or audibleindicator. When the pressure is within the first pressure range, outputdevice 150 presents a ready light and a beep that is emitted at onesecond intervals. When the pressure is above the first pressure range,output device 150 presents an “over pressure” display and a beep that isemitted at half-second intervals. Alternatively, output device 150 maypresent any indication to the operator that enables surgical system 100to function as described herein.

In the exemplary embodiment, when the applied pressure is within thepredetermined pressure range, the operator presses foot pedal 160 downto initiate transmission of the control signal to activate a weld cycle.More specifically, surgical generator 110 transmits the control signalto handpiece 120 upon determining and/or identifying that the appliedpressure is within the first pressure range and/or determining and/oridentifying that foot pedal 160 is pressed down. In one embodiment, thecontrol signal is transmitted to handpiece 120 upon receiving the firstindication that the applied pressure is within the first pressure rangeand then the second indication that foot pedal 160 is pressed second. Inanother embodiment, the control signal is transmitted to handpiece 120upon receiving the second indication that foot pedal 160 is pressed downand then the first indication that the applied pressure is within thefirst pressure range.

In the exemplary embodiment, vibrating mechanism 290 receives 340 thecontrol signal to activate a weld cycle and generates 350 vibratoryenergy upon receiving the control signal. The vibratory energy istransferred through horn 180 and end effector 190 to the surgicalimplement. The vibratory energy propagates through the surgicalimplement to vibrate the surgical implement and an adjacent surgicalimplement, which generates heat and a weld therebetween.

During operation of handpiece 120 in the active weld cycle, outputdevice 150 presents an indication of the active weld cycle to theoperator. For example, in one embodiment, an audio output devicepresents an audible tone indicative of the active weld cycle. In theexemplary embodiment, the active weld cycle stops when the weld iscomplete. More specifically, surgical generator 110 determines and/oridentifies that the weld is complete based on a predetermined amount ofenergy or work applied by handpiece 120, and stops transmission of thecontrol signal and/or transmits a second control signal to stop theactive weld cycle when the weld is complete. In the exemplaryembodiment, the amount of energy applied to the surgical implement isapproximately 100 Joules (J). Alternatively, surgical generator 110 mayapply any amount of energy that enables surgical system 100 to functionas described herein.

FIG. 4 is a cross-sectional view of another exemplary handpiece 420,which may be removably coupled to surgical generator 110 (shown in FIG.1). Alternatively, surgical generator 110 may be integrated withhandpiece 420. In the exemplary embodiment, handpiece 420 includes anouter housing 470, a horn 480 extending longitudinally from outerhousing 470, an end effector 490 coupled to horn 480, and a sheath (notshown) coupled to outer housing 470 and extending about and spacedradially from horn 480 and/or end effector 490. In the exemplaryembodiment, horn 480 and/or end effector 490 are sized and/or configuredto slide within the sheath. In at least some embodiments, end effector490 is integrated with horn 480.

In the exemplary embodiment, handpiece 420 is useable to affect one ormultiple surgical implements during a surgery. More specifically,handpiece 420 applies vibratory energy, such as ultrasonic energy, toone or more of the surgical implements to form a weld between thesurgical implements. Alternatively, handpiece 420 may apply any energythat enables surgical generator 110 and/or handpiece 420 to function asdescribed herein.

In the exemplary embodiment, handpiece 420 is configured to provide anergonomic interaction with the operator. Other shapes and/or sizes ofhandpiece 420 may be included in other surgical system embodiments. Inat least some embodiments, handpiece 420 is configured to interact withand/or be utilized by a robotic arm for robotic and/or remote control ofhandpiece 420.

In the exemplary embodiment, outer housing 470 houses at least an innerhousing 500, a positional sensor 510 extending longitudinally or axiallybetween an end cap of inner housing 500 and an end cap of outer housing470, and a biasing mechanism 520 moveable between an unflexed or homeposition and a flexed position. As a first force and/or pressure appliedto positional sensor 510 and/or biasing mechanism 520 generallyincreases, in the exemplary embodiment, biasing mechanism 520 movestoward the flexed position. Conversely, as the first pressure applied topositional sensor 510 and/or biasing mechanism 520 generally decreases,in the exemplary embodiment, biasing mechanism 520 moves toward the homeposition.

In the exemplary embodiment, the first pressure is associated with aforce and/or pressure between end effector 490 and a surgical implementin contact with end effector 490, which, in turn, directly applies aforce and/or pressure to horn 480. In the exemplary embodiment, biasingmechanism 520 is a coil spring configured to compress as the firstpressure increases and/or expand as the first pressure decreases.Alternatively, any type of biasing mechanism 520 may be used thatenables handpiece 420 to function as described herein.

In the exemplary embodiment, positional sensor 510 is configured todetect the first pressure applied to positional sensor 510 and/orbiasing mechanism 520 and transmit to surgical generator 110 a pressuresignal associated with and/or indicative of the first pressure. Morespecifically, positional sensor 510 detects a longitudinal or axialcompression and/or extension of positional sensor 510 and/or biasingmechanism 520 and determines the first pressure based at least in parton the axial compression and/or extension. In the exemplary embodiment,positional sensor 510 is a linear variable differential transformerand/or a Hall effect sensor. Alternatively, positional sensor 510 may beany sensor that enables handpiece 420 to function as described herein.

In the exemplary embodiment, outer housing 470 defines a cavity thereinthat is sized and/or configured such that inner housing 500 is retainedwithin outer housing 470. More specifically, outer housing 470 and/orinner housing 500 includes at least one retaining mechanism 550configured to prevent and/or limit inner housing 500 from moving awayfrom positional sensor 510 and/or biasing mechanism 520 beyond apredetermined position. In the exemplary embodiment, retaining mechanism550 is a step that generally complements a flange extending radiallyoutward from the end cap of inner housing 500. Alternatively, any typeof retaining mechanism 550 may be used that enables handpiece 420 tofunction as described herein.

In the exemplary embodiment, inner housing 500 houses at least a portionof horn 480 and at least a portion of the transducer system or, morespecifically, vibrating mechanism 590 coupled to horn 480. In theexemplary embodiment, vibrating mechanism 590 is a piezoelectric stackthat is configured to generate vibratory energy (e.g., ultrasonicenergy) upon receiving a control signal to activate a weld cycle. In theexemplary embodiment, horn 480 is configured to transmit the vibratoryenergy to an operative site. More specifically, horn 480 is coupleableto end effector 490 such that the vibratory energy is transmitted to endeffector 490 through horn 480. Alternatively, the vibratory energy maybe transmitted to the operative site using any mechanism that enableshandpiece 420 to function as described herein.

The embodiments described herein relate generally to medical devicesand, more particularly, to an ultrasonic handpiece. The ultrasonichandpieces described herein enable monitoring forces and/or pressuresapplied to the handpiece, its components, and/or a surgical implement.As such, the handpieces described herein facilitate creating effectiveand/or reliable welds, thereby improving a repair, stabilization, and/orhealing time associated with the patient.

Exemplary embodiments of ultrasonic handpieces are described above indetail. The methods and systems are not limited to the specificembodiments described herein, but rather, components of systems and/orsteps of the method may be utilized independently and separately fromother components and/or steps described herein. Each method step andeach component may also be used in combination with other method stepsand/or components. Although specific features of various embodiments maybe shown in some drawings and not in others, this is for convenienceonly. Any feature of a drawing may be referenced and/or claimed incombination with any feature of any other drawing.

This written description uses examples to disclose the embodiments,including the best mode, and also to enable any person skilled in theart to practice the embodiments, including making and using any devicesor systems and performing any incorporated methods. The patentable scopeof the disclosure is defined by the claims, and may include otherexamples that occur to those skilled in the art. Such other examples areintended to be within the scope of the claims if they have structuralelements that do not differ from the literal language of the claims, orif they include equivalent structural elements with insubstantialdifferences from the literal language of the claims.

1-20. (canceled)
 21. A method of operating a handheld medical device,said method comprising: detecting a first pressure applied to a horn ofthe handheld medical device when the horn is pressed against a firstsurgical implement; determining when the first pressure is within apredetermined pressure range indicating that the first pressure issuitable for securing the first surgical implement to a second surgicalimplement; generating energy when the first pressure has remained withinthe predetermined pressure range for at least a predetermined durationof time; and applying the energy through the horn to the first surgicalimplement to secure the first surgical implement to the second surgicalimplement.
 22. The method of claim 21, further comprising inhibiting thegeneration of energy when the first pressure is outside thepredetermined pressure range.
 23. The method of claim 21, furthercomprising: determining when the first surgical implement is secured tothe second surgical implement; and stopping the generation of energyafter determining the first surgical implement is secured to the secondsurgical implement.
 24. The method of claim 23, further comprisingproviding an indication to a user when the first surgical implement issecured to the second surgical implement.
 25. The method of claim 23,wherein said determining when the first surgical implement is secure tothe second surgical implement comprises determining when a predeterminedamount of energy has been applied to the first surgical implement by thehandheld medical device.
 26. The method of claim 21, wherein thepredetermined duration of time is 2 seconds.
 27. The method of claim 21,wherein the energy generated is vibratory energy.
 28. The method ofclaim 21, further comprising receiving a user input, wherein saidgenerating energy further comprises generating energy when the firstpressure has remained within the predetermined pressure range for atleast a predetermined duration of time and the user input has beenreceived.
 29. The method of claim 21, further comprising: identifyingthe handheld medical device based on an identifier associated with thehandheld medical device; and retrieving at least one setting for thehandheld medical device based on the identifier.
 30. The method of claim29, wherein the at least one setting includes the predetermined pressurerange.
 31. The method of claim 30, wherein the at least one settingfurther includes the predetermined duration of time.
 32. A controllerfor use with a handheld medical device, the controller comprising: aprocessor; and a memory device having encoded thereon computer-readableinstructions that are executable by the processor to perform functionscomprising: